Maria Isychou
About Maria Isychou
Professional Background in Pharmaceuticals
Maria Isychou has amassed over 13 years of experience in the pharmaceutical industry, holding multiple roles that span clinical trial management, line management, and vendor oversight. Her career began in Sydney, Australia, where she worked at PAREXEL as a Clinical Trial Assistant and later as a Clinical Research Associate. She also held significant roles at Amgen, including Clinical Operations Manager and Head of the FSP Department. Her experience includes positions at Arena Pharmaceuticals and her current role at BeiGene in Basel, Switzerland.
Educational Background and Certifications
Maria Isychou holds a Bachelor of Science (B.Sc.) with a major in Pharmacology from the University of Sydney, completed between 2002 and 2006. Furthering her education, she achieved a Project Management Professional (PMP) certificate from the Project Management Institute (PMI) after studying at the Institute of Project Management from 2014 to 2015. This robust educational background complements her extensive experience in clinical operations and trial management.
Leadership Roles in Clinical Operations
Throughout her career, Maria Isychou has held several leadership positions, showcasing her robust management and oversight skills. At Amgen, she served as FSP Line Manager for CRA, CTA & Contract Specialists, and later as the a.i. Head of the FSP Department in Greece. Moving to Arena Pharmaceuticals, she became the Senior Clinical Trial Manager and Vendor Oversight Lead. Currently, she is the Associate Director of Clinical Operations at BeiGene, where she continues to leverage her expertise in clinical trials and team development.
Strong Expertise in Clinical Trials
Maria Isychou brings sound knowledge and extensive expertise in clinical trials and clinical operations to her roles. She has been involved in both audits and inspections and has demonstrated strong leadership in risk management and issue resolution. Her work in dynamic, diverse, and fast-paced environments across Australia and Europe has equipped her with critical thinking and problem-solving abilities, making her a valuable asset in clinical trial management and operations.